Report Coordinator I - Remote
Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you’re a recent college graduate or seeking your next career opportunity, it’s time to discover your future at Altasciences. We are better together and together We Are Altasciences.
About The Role
The primary responsibility of the Report Coordinator will be to write research reports for studies performed at APC, both GLP and non-GLP studies. The Report Coordinator will ensure that all reports accurately depict the conduct of the study according to the raw data and protocol and will require a reasonable amount of supervision. The Report Coordinator will assist the Study Director throughout the lifetime of the study report from study termination through report finalization.
What You'll Do Here
- Maintain competency in the current APC Standard Operating Procedures (SOPs), and GLP regulations.
- Review draft protocols for reporting requirements, formatting, content, and clarity.
- Write the materials and methods section for reports by closely following the protocol and by verifying documented procedures.
- Add tables to reports after verifying that review of data has been performed for non-GLP studies and QA review has been performed on GLP studies.
- Work closely with Study Directors and APC personnel to resolve report writing or data clarity issues.
- Review internal Contributing Scientist Reports (CSR) for APC format and style guideline requirements.
- Peer review of the material and methods, tables, and deviation section to ensure conformity to protocol and SOP requirements.
- Assure that reports written meet APC standards for formatting, clarity, accuracy and completeness.
- Review the Report/QA schedule of all non-clinical laboratory studies conducted and maintain timelines.
- Compile all reports for shipment including interim, draft and final reports.
What You'll Need To Succeed
- Bachelor's degree (B.A./B.S.) from four year college or university; or one to two years related experience and/or training; or equivalent combination of education and experience.
- Affiliation and/or training with a relevant professional organization, is desirable.
- This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.
- Skills: Problem solving/analysis, project management, customer/client focus, collaboration skills, communication proficiency, ethical conduct, time management, and thoroughness.
Benefits
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences’ Benefits Package Includes
- Health/Dental/Vision Insurance Plans
- 401(k)/RRSP with Employer Match
- Paid Vacation and Holidays
- Paid Sick and Bereavement Leave
- Employee Assistance & Telehealth Programs
- Telework when applicable
Altasciences’ Incentive Programs Include
- Training & Development Programs
- Employee Referral Bonus Program
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Other details
- Job Family P-4
- Pay Type Hourly
- Columbia, MO, USA